口腔鳞状细胞癌3号染色体短臂杂合性缺失:3p25-ter区域杂合性缺失与临床和组织学特征的关系

N. Uzawa, D. Akanuma, A. Negishi, T. Amagasa, Mitsuaki Yoshida
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引用次数: 5

摘要

细胞遗传学和分子生物学研究表明,一个可能在口腔鳞状细胞癌变过程中起重要作用的肿瘤抑制基因位于3号染色体短臂(3p)上。我们利用5个微卫星标记分析了17例口腔鳞状细胞癌(OSCCs)的3p杂合性缺失(LOH),特别是3p25 -pter区域,并构建了该染色体短臂的缺失图谱。17例肿瘤中有9例(53%)在一个或多个位点检测到LOH。这些区域的LOH在晚期OSCCs中更为常见,可能与肿瘤进展有关。我们的数据支持这样一种观点,即促进口腔鳞状细胞癌进展的肿瘤抑制基因之一位于3p25 -pter上。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Loss of Heterozygosity on the Short Arm of Chromosome 3 in Oral Squamous Cell Carcinomas : Relationship between loss of heterozygosity on 3p25-ter region and clinical and histological features
Cytogenetic and molecular studies have indicated that a putative tumor suppresor gene (s), which may play an important role in oral squamous cell carcinogenesis, is located on the short arm of chromosome 3 (3 p). We analyzed loss of heterozygosity (LOH) on 3 p, especially the 3 p25-pter region, in 17 oral squamous cell carcinomas (OSCCs) with the use of 5 microsatellite markers and constructed a deletion map for this chromosome arm. LOH at one or more loci was detected in 9 of 17 (53%) tumors. LOH on these region was more common in advanced OSCCs and may be associated with tumor progression. Our data support the notion that one of tumor suppressor gene (s) contributing to the progression of oral squamous cell carcinoma resides on 3 p25-pter.
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